{
  "id": 14918,
  "label": "amelogenesis imperfecta hypomaturation type 2A4",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0013906",
  "properties": {
    "xrefs": [
      "DOID:0110062",
      "GARD:0015847",
      "MEDGEN:766744",
      "OMIM:614832",
      "UMLS:C3553830"
    ],
    "synonyms": [
      "AI2A4",
      "ODAPH amelogenesis imperfecta",
      "amelogenesis imperfecta caused by mutation in ODAPH",
      "amelogenesis imperfecta, type IIA4",
      "amelogenesis imperfecta, hypomaturation type, IIA4"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0006858",
        "name": "mouth disorder"
      }
    ],
    "definition": "Any amelogenesis imperfecta in which the cause of the disease is a mutation in the ODAPH gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16024,
      "label": "amelogenesis imperfecta type 2",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19324
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0008349",
          "ICD9:520.5",
          "MEDGEN:97994",
          "MESH:C536606",
          "Orphanet:100033",
          "SCTID:109475005",
          "UMLS:C0399372"
        ],
        "synonyms": [
          "hypomaturation amelogenesis imperfecta",
          "amelogenesis imperfecta hypomaturation type"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0006858",
            "name": "mouth disorder"
          }
        ]
      },
      "child_count": 7,
      "reference_id": "MONDO:0015048"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16024,
      "label": "amelogenesis imperfecta type 2"
    }
  ]
}